Trials / Completed
CompletedNCT00881959
Study of Root Coverage With Acellular Dermal Matrix: Puros® Dermis Versus Alloderm®
Multi-center, Post-market, Prospective, Randomized, Examiner-Only-Masked Study of Root Coverage With Acellular Dermal Matrix: Puros® Dermis Versus Alloderm®
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 80 (actual)
- Sponsor
- Zimmer Biomet · Industry
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of the study is to evaluate whether clinical parameters for Puros Dermis are, at minimum, equivalent when compared to AlloDerm, the current industry standard, for the treatment of single, non-adjacent Miller's Class I or II gingival recession.
Detailed description
This is a prospective, Post-market, Randomized, Examiner-Only Masked multi-center study to evaluate whether clinical parameters for Puros Dermis are at minimum, equivalent when compared to Alloderm, the current industry standard for the treatment of single, non-adjacent Miller's Class I or II gingival recession.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Puros® Dermis versus Alloderm® | Puros Dermis and Alloderm (both Allograft Tissue Matrix) |
Timeline
- Start date
- 2009-08-01
- Primary completion
- 2012-04-01
- Completion
- 2012-06-01
- First posted
- 2009-04-15
- Last updated
- 2015-05-27
- Results posted
- 2015-05-27
Locations
4 sites across 1 country: United States
Source: ClinicalTrials.gov record NCT00881959. Inclusion in this directory is not an endorsement.